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N/A N=36 Randomized Single-blind Other

Topical Proparacaine Eye Drops to Improve the Experience of Patients Undergoing Intravitreal Injections

Age-related Macular Degeneration · Diabetic Macular Edema · Injection Site · Injection Site Infection · Pain, Postoperative

Enrolled (actual)
36
Serious AEs
0.0%
Results posted
Jun 2019
Primary outcome: Primary: Number of Study Participants With Positive Conjunctival Culture — 1; 1 Participants — p=0.28

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Proparacaine (Drug); Conjunctival culture (Procedure)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Mayo Clinic
Primary completion
Feb 2018

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Study Participants With Positive Conjunctival Culture
1; 1 0.28
PRIMARY
Pain at the Time of Injection
2; 1 0.25
SECONDARY
Residual Pain From Intravitreal Injection
1; 0 0.86
SECONDARY
Overall Impression of Visit for Intravitreal Injection
0; 0 0.48
SECONDARY
Impression of Pre-injection Preparations
0; 0 0.76
SECONDARY
Comfort With Intravitreal Injection Standard Procedure
0; 0 0.31
SECONDARY
Expectation Intravitreal Injection Will Have Negative Consequences on Subject Health
0; 0 0.18
SECONDARY
Expectation the Injection Will Contribute to Curing/Improving Eye Condition
8; 10 0.67

Summary

The specific aims of this study are to compare patient experience with and without a proparacaine drop after povidone iodine.

Eligibility Criteria

Inclusion Criteria

  • patients undergoing intravitreal injection who do not have active eye infections
  • greater than 18 years of age

Exclusion Criteria

  • patients younger than 18 years of age
  • patients with active eye infections
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02951351). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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